Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs180177042 | 0.807 | 0.280 | 7 | 140749365 | missense variant | A/C;T | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs180177042 | 0.807 | 0.280 | 7 | 140749365 | missense variant | A/C;T | snv | 7 |